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巨大胃幼年性息肉病合并间歇性胃出口梗阻:一例报告

Massive Gastric Juvenile Polyposis Associated With Intermittent Gastric Outlet Obstruction: A Case Report.

作者信息

Linardoutsos Dimitrios, Mela Evgenia, Triantafyllou Stamatina, Machairas Anastasios

机构信息

First Propaedeutic Department of Surgery, Hippocration General Hospital, National and Kapodistrian University of Athens, School of Medicine, Athens, GRC.

Department of Surgery, Metropolitan General Hospital, Athens, GRC.

出版信息

Cureus. 2024 Jun 6;16(6):e61792. doi: 10.7759/cureus.61792. eCollection 2024 Jun.

DOI:10.7759/cureus.61792
PMID:38975412
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11227121/
Abstract

Juvenile polyposis syndrome is a condition distinguished by numerous hyperproliferative polyps that can affect the entire gastrointestinal tract, though they are uncommon in the stomach. We report a rare case of a 70-year-old woman with a three-year history of epigastric pain and severe bloating who was referred to our department for gastric outlet obstruction due to massive gastric juvenile polyps also causing gastroparesis. The patient was successfully treated with a total gastrectomy.

摘要

幼年性息肉病综合征是一种以大量增生性息肉为特征的疾病,可累及整个胃肠道,不过在胃中较为少见。我们报告一例罕见病例,一名70岁女性,有三年上腹部疼痛和严重腹胀病史,因大量胃幼年性息肉导致胃出口梗阻并伴有胃轻瘫而转诊至我科。该患者接受全胃切除术后成功治愈。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc48/11227121/29bc2fd2374a/cureus-0016-00000061792-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc48/11227121/ddc243fd93ae/cureus-0016-00000061792-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc48/11227121/88d702af6f72/cureus-0016-00000061792-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc48/11227121/29bc2fd2374a/cureus-0016-00000061792-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc48/11227121/ddc243fd93ae/cureus-0016-00000061792-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc48/11227121/88d702af6f72/cureus-0016-00000061792-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc48/11227121/29bc2fd2374a/cureus-0016-00000061792-i03.jpg

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本文引用的文献

1
Juvenile polyposis syndrome with gastric and duodenal polyposis presenting with refractory anemia and protein-leakage gastroenteropathy in a patient with SMAD4 mutation: a case report.一名患有SMAD4突变的青少年息肉病综合征患者,伴有胃和十二指肠息肉病,表现为难治性贫血和蛋白丢失性胃肠病:病例报告
Surg Case Rep. 2024 Jan 9;10(1):11. doi: 10.1186/s40792-023-01796-4.
2
Massive Gastric Juvenile Polyposis: A Clinicopathologic Study Using SMAD4 Immunohistochemistry.巨大胃幼年性息肉病:一项使用SMAD4免疫组织化学的临床病理研究
Am J Clin Pathol. 2017 Apr 1;147(4):390. doi: 10.1093/ajcp/aqx015.
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ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes.
ACG 临床指南:遗传性胃肠道癌综合征的基因检测与管理。
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Upper tract juvenile polyps in juvenile polyposis patients: dysplasia and malignancy are associated with foveolar, intestinal, and pyloric differentiation.幼年性息肉病患者的上消化道幼年性息肉:发育异常和恶性肿瘤与小凹、肠型和幽门型分化相关。
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High proportion of large genomic deletions and a genotype phenotype update in 80 unrelated families with juvenile polyposis syndrome.80个无关的青少年息肉病综合征家庭中基因组大片段缺失的高比例及基因型-表型更新
J Med Genet. 2007 Nov;44(11):702-9. doi: 10.1136/jmg.2007.052506. Epub 2007 Sep 14.
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Juvenile polyposis: massive gastric polyposis is more common in MADH4 mutation carriers than in BMPR1A mutation carriers.青少年息肉病:与BMPR1A突变携带者相比,MADH4突变携带者中更常见大量胃息肉。
Hum Genet. 2002 Jul;111(1):108-11. doi: 10.1007/s00439-002-0748-9. Epub 2002 Jun 13.
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Juvenile polyposis--a precancerous condition.青少年息肉病——一种癌前病变状态。
Histopathology. 1988 Dec;13(6):619-30. doi: 10.1111/j.1365-2559.1988.tb02093.x.
10
Familial juvenile polyposis of the stomach.
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